Allele Registry

Canonical Allele Identifier: PA2826946882

Gene: F9 HGNC NCBI

ClinVar Allele:

25620

ClinVar RCV:

RCV000011327

ClinVar Variation:

10581

HGVS (amino-acid)	Matching Registered Transcripts
NP_001300842.1:p.Gly122Ala	CA255334 NM_001313913.2:c.365G>C